Canonical Allele Identifier: CA389147321
Gene: RNASE3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.21360308C>G (hg19) chr14:g.20892149C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20892149C>G , CM000676.2:g.20892149C>G GRCh38
NC_000014.8:g.21360308C>G , CM000676.1:g.21360308C>G GRCh37
NC_000014.7:g.20430148C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000304639.4:c.463C>G MANE Select ENSP00000302324.3:p.His155Asp
ENST00000304639.3:c.463C>G ENSP00000302324.3:p.His155Asp
NM_002935.2:c.463C>G NP_002926.2:p.His155Asp
XR_110261.2:n.209-16406G>C
XR_110261.3:n.726-16406G>C
NM_002935.3:c.463C>G MANE Select NP_002926.2:p.His155Asp
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